PLANT BIOLOGY
ANIMAL BIOLOGY
SUBSCRIPTION
E-SUBSCRIPTION
 
MAP
MAIN PAGE

 

 

 

 

doi: 10.15389/agrobiology.2023.2.260eng

UDC: 636.4:619:578

Acknowledgements:
Carried out according to the State assignment No. FGUG-2022-0009

 

ATYPICAL PORCINE PESTIVIRUS (Pestivirus K) — A NEW CHALLENGE FOR PIG FARMING (review)

A.M. Anoyatbekova, A.G. Yuzhakov, M. Anoyatbekov, T.I. Aliper,
A.M. Gulyukin

Federal Scientific Centre Skryabin and Kovalenko All-Russian Research Institute of Experimental Veterinary RAS, 24/1, Ryazanskii Prosp., Moscow, 109428 Russia, e-mail aafshona@mail.ru (✉ corresponding author), nton_oskol@mail.ru, anoyatbekov@list.ru,
aliper@narvac.com, admin@viev.ru

ORCID:
Anoyatbekova A.M. orcid.org/0000-0002-6579-779X
Aliper T.I. orcid.org/0000-0003-2696-1363
Yuzhakov A.G. orcid.org/0000-0002-9354-6824
Gulyukin A.M. orcid.org/0000-0003-2160-4770
Anoyatbekov M. orcid.org/0000-0002-0180-0574

Final revision received August 22, 2022
Accepted September 7, 2022

Pestiviruses are highly variable RNA viruses of the genus Pestivirus, family Flaviviridae. The genus Pestivirus includes 11 species, from Pestivirus A to Pestivirus K (B.G. Orlyankin et al., 2020; D.B. Smith et al., 2017; A.M.Q. King et al., 2018). In the infectious pathologies of pigs, pestiviruses are highly important due to significant economic losses. Over the past two decades, many previously undescribed pestiviruses have been found in domestic pigs and wild boars. Due to the tendency to rapid spread, they can cause a serious threat to pig production. In 2015, in the framework of the Porcine Reproductive and Respiratory Syndrome Virus genetic diversity project in the US, an atypical porcine pestivirus (Pestivirus K) was first identified in blood serum by metagenomic sequencing. Initially, it was assumed that pigs infected with atypical pestivirus did not show clinical signs of the disease. However, the experiments on the study of atypical pestivirus infectious properties showed that the pestivirus causes congenital tremor (CT) type A-II in piglets (B.L. Arruda et al., 2016; A. de Groof et al., 2016; A. Postel et al., 2017). Adult domestic pigs and wild boars are also susceptible to the virus. Atypical porcine pestivirus is transmitted vertically and horizontally and is widespread in many countries of Europe, America and Asia. In Russia, atypical porcine pestivirus has not been diagnosed in pigs. The phylogenetic analysis of the genome of all known isolates revealed 3 genetic groups (1st-3d) and seven subgenotypes within the 1st genetic group (1.1-1.7) of the virus (F. Yuan et al., 2021). The first genetic group includes all isolates identified in the USA, Europe and several isolates from China. The second and third genetic groups are isolates from China only. The circulation of atypical porcine pestivirus in herds can complicate the differential diagnosis of classical swine fever, due to some similarity of symptoms, the congenital tremor particularly. Consequently, the knowledge of the epidemiology of the atypical porcine pestivirus in different geographic regions will help optimization of its control and prevention of spreading. The review covers current data of the etiology, distribution, clinical manifestations, diagnosis and prevention of the atypical porcine pestivirus infection.

Keywords: atypical porcine pestivirus, identification, differential diagnosis, congenital tremor, pigs, classical swine fever, diseases prevention.

 

REFERENCES

  1. Glotov A.G., Glotova T.I. Atypical bovine pestiviruses (review). Sel'skokhozyaistvennaya biologiya [Agricultural Biology], 2015, 50(4): 399-408 CrossRef
  2. Blome S., Staubach C., Henke J., Carlson J., Beer M. Classical swine fever — an updated review. Viruses, 2017, 9(4): 86 CrossRef
  3. Sergeev V.A., Orlyankin B.G., Alekseev K.P. Zaberezhnyy A.D., Aliper T.I., Nepoklonov E.A. Veterinariya, 2018, 4: 3-11 (in Russ.).
  4. Orlyankin B.G., Sergeev V.A., Aliper T.I., Nepoklonov E.A. Veterinariya, 2020, 6: 3-9 CrossRef (in Russ.).
  5. Kirkland P.D., Le Potier M.F. Finlaison D. Pestiviruses. In: Diseases of swine. J.J. Zimmerman, L.A. Karriker, A. Ramirez, K.J. Schwartz, G.W. Stevenson, J. Zhang (eds.). John Wiley & Sons, Inc., 2019: 622-640 CrossRef
  6. Fernelius A.L., Amtower W.C., Lambert G., McClurkin A.W., Matthews P.J. Bovine viral diarrhea virus in swine: characteristics of virus recovered from naturally and experimentally infected swine. Can. J. Comp. Med., 1973, 37(1): 13-20.
  7. Terpstra C., Wenswoort G. Natural infections of pigs with bovine viral diarrhoea virus associated with signs resembling swine fever. Res. Vet. Sci., 1988, 45: 137-142.
  8. Deng Y., Sun C.Q., Cao S.J., Lin T., Yuan S.S., Zhang H.B., Zhai S.L., Huang L., Shan T.L., Zheng H., Wen X.T., Tong G.Z. High prevalence of bovine viral diarrhea virus 1 in Chinese swine herds. Veterinary Microbiology, 2012, 159(3-4): 490-493 CrossRef
  9. Almeida H.M.S., Gatto I.R.H., Santos A.C.R., Pereira D.A., Nascimento K.A., Baraldi T.G., Mechler M.L., de Oliveira L.G. Bovine viral diarrhea virus infections in pigs: why is this situation important for Brazilian herds? Arquivos do Instituto Biológico, 2018, 84: e0322016 CrossRef
  10. Rosell R., Cabezón O., Pujols J., Domingo M., Muñoz I., Núñez J.I., Ganges L. Identification of a porcine pestivirus as a border disease virus from naturally infected pigs in Spain. Veterinary Record, 2014, 174(1): 18 CrossRef
  11. Kawanishi N., Tsuduku S., Shimizu H., Ohtani Y., Kameyama K., Yamakawa M., Tsutsui T., Matsuura K., Ohashi S., Isobe T., Yamada S. First isolation of border disease virus in Japan is from a pig farm with no ruminants. Veterinary Microbiology, 2014, 171(1-2): 210-214 CrossRef
  12. Decaro N., Mari V., Lucente M.S., Sciarretta R., Moreno A., Armenise C., Losurdo M., Camero M., Lorusso E., Cordioli P., Buonavoglia C. Experimental infection of cattle, sheep and pigs with Hobi-like pestivirus. Veterinary Microbiology, 2012, 155(2-4): 165-171 CrossRef
  13. Bauermann F.V., Falkenberg S.M., Decaro N., Flores E.F., Ridpath J.F. Experimental infection of calves, sheep, goats and pigs with HoBi-like viruses by direct inoculation or exposure to persistently infected calves. Veterinary Microbiology, 2015, 181(3-4): 289-293 CrossRef
  14. Kirkland P.D., Frost M.J., Finlaison D.S., King K.R., Ridpath J.F., Gu X. Identification of a novel virus in pigs — Bungowannah virus: a possible new species of pestivirus. Virus Res., 2007, 129(1): 26-34 CrossRef
  15. Kirkland P.D., Read A.J., Frost M.J., Finlaison D.S. Bungowannah virus — a probable new species of pestivirus — what have we found in the last 10 years? Animal Health Research Review, 2015, 16(1): 60-63 CrossRef
  16. Lamp B., Schwarz L., Högler S., Riedel C., Sinn L., Rebel-Bauder B., Weissenböck H., Ladinig A., Rümenapf T. Novel Pestivirus species in pigs, Austria. Emerging Infectious Disease, 2017, 23(7): 1176-1179 CrossRef
  17. Kiesler A., Seitz K., Schwarz L., Buczolich K., Petznek H., Sassu E., Lamp, B. Clinical and Serological Evaluation of LINDA Virus Infections in Post-Weaning Piglets. Viruses, 2019, 11(975): 975 CrossRef
  18. Stenberg H., Jacobson M., Malmberg M. A review of congenital tremor type A-II in piglets. Animal Health Research Review, 2020, 21(1): 84-88 CrossRef
  19. Done J.T. Congenital nervous diseases of pigs: a review. Laboratory Animals, 1968, 2(2): 207-218 CrossRef
  20. Done J.T., Woolley J., Upcott D.H., Hebert C.N. Porcine congenital tremor type AII: spinal cord morphometry. British Veterinary Journal, 1986, 142(2): 145-150 CrossRef
  21. Gatto I.R.H., Sonálio K., de Oliveira L.G. Atypical Porcine Pestivirus (APPV) as a new species of Pestivirus in pig production. Frontiers in Veterinary Science, 2019, 6: 35 CrossRef
  22. Dall Agnol A.M., Alfieri A.F., Alfieri A.A. Pestivirus K (Atypical Porcine Pestivirus): update on the virus, viral infection, and the association with congenital tremor in newborn piglets. Viruses, 2020, 12: 903 CrossRef
  23. Hause B.M., Collin E.A., Peddireddi L., Yuan F., Chen Z., Hesse R.A., Gauger P.C., Clement T., Fang Y., Anderson G. Discovery of a novel putative atypical porcine pestivirus in pigs in the USA. Journal of General Virology, 2015, 96(10): 2994-2998 CrossRef
  24. Arruda B.L., Arruda P.H., Magstadt D.R., Schwartz K.J., Dohlman T., Schleining J.A., Patterson A.R., Visek C.A., Victoria J.G. Identification of a divergent lineage porcine pestivirus in nursing piglets with congenital tremors and reproduction of disease following experimental inoculation. PLoS ONE, 2016, 11(2): e0150104 CrossRef
  25. Wu Z., Ren X., Yang L., Hu Y., Yang J., He G., Zhang J., Dong J., Sun L., Du J., Liu L., Xue Y., Wang J., Yang F., Zhang S., Jina Q. Virome analysis for identification of novel mammalian viruses in bat species from Chinese provinces. Journal of Virology, 2012, 86(20): 10999-1012 CrossRef
  26. Tautz N., Tews B.A., Meyers G. The molecular biology of Pestiviruses. Advances in Virus Research, 2015, 93: 47-160 CrossRef
  27. Smith D.B., Meyers G., Bukh J., Gould E.A., Monath T., Scott Muerhoff A., Pletnev A., Rico-Hesse R., Stapleton J.T., Simmonds P., Becher P. Proposed revision to the taxonomy of the genus Pestivirus, family Flaviviridae. Journal of General Virology, 2017, 98(8): 2106-2112 CrossRef
  28. King A.M.Q., Lefkowitz E.J., Mushegian A.R., Adams M.J., Dutilh B.E., Gorbalenya A.E., Harrach B., Harrison R.L., Junglen S., Knowles N.J., Kropinski A.M., Krupovic M., Kuhn J.H, Nibert M.L., Rubino L., Sabanadzovic S., Sanfaçon H., Siddell S.G., Simmonds P., Varsani A., Zerbini F.M., Davison A.J. Changes to taxonomy and the International Code of Virus Classification and Nomenclature ratified by the International Committee on Taxonomy of Viruses. Archives of Virology, 2018, 163(9): 2601-2631 CrossRef
  29. Anoyatbekova A.M., Alexeenkova S.V., Yurov K.P. Identification of the emergent pestivirus infections of small ruminants in Tajikistan. IOP Conf. Series. Erath and Environmental Science, 2020, 548(2): e022066 CrossRef
  30. Postel A., Smith D.B., Becher P. Proposed update to the taxonomy of Pestiviruses: eight additional species within the genus Pestivirus, family Flaviviridae. Viruses, 2021, 13(8): 1542 CrossRef
  31. de Groof A., Deijs M., Guelen L., van Grinsven L., van Os-Galdos L., Vogels W., Derks C., Cruijsen T., Geurts V., Vrijenhoek M., Suijskens J., van Doorn P., van Leengoed L., Schrier C., van der Hoek L. Atypical porcine pestivirus: a possible cause of congenital tremor type A-II in newborn piglets. Viruses, 2016, 8(10): 271 CrossRef
  32. Sutton K.M., Lahmers K.K., Harris S.P., Wijesena H.R., Mote B.E., Kachman S.D., Borza T., Ciobanu D.C. Detection of atypical porcine pestivirus genome in newborn piglets affected by congenital tremor and high preweaning mortality. Journal of Animal Science, 2019, 97(10): 4093-4100 CrossRef
  33. Gatto I.R.H., Arruda P.H., Visek C.A., Victoria J.G., Patterson A.R., Krull A.C., Schwartz K.J., de Oliveira L.G., Arruda B.L. Detection of atypical porcine pestivirus in semen from commercial boar studs in the United States. Transboundary and Emerging Diseases, 2018, 65(2): e339-e343 CrossRef
  34. Chen F., Knutson T.P., Braun E., Jiang Y., Rossow S., Marthaler D.G. Semi-quantitative duplex RT-PCR reveals the low occurrence of porcine Pegivirus and atypical porcine Pestivirus in diagnostic samples from the United States. Transboundary and Emerging Diseases, 2019, 66(3): 1420-1425 CrossRef
  35. Schwarz L., Riedel C., Hogler S., Sinn L.J., Voglmayr T., Wochtl B., Dinhopl N., Rebel-Bauder B., Weissenbock H., Ladinig A., Rumenapf T., Lamp B. Congenital infection with atypical porcine pestivirus (APPV) is associated with disease and viral persistence. Veterinary Research, 2017, 48(1): 1 CrossRef
  36. Yuan J., Han Z., Li J., Huang Y., Yang J., Ding H., Zhang J., Zhu M., Zhang Y., Liao J., Zhao M., Chen J. Atypical porcine pestivirus as a novel type of pestivirus in pigs in China. Front. Microbiol., 2017, 8: 862 CrossRef
  37. Yan X.L., Li Y.Y., He L.L., Wu J.L., Tang X.Y., Chen G.H., Mai K.J., Wu R.T., Li Q.N., Chen Y.H., Sun Y., Ma J.Y. 12 novel atypical porcine pestivirus genomes from neonatal piglets with congenital tremors: A newly emerging branch and high prevalence in China. Virology, 2019, 533: 50-58 CrossRef
  38. Xie Y., Wang X., Su D., Feng J., Wei L., Cai W., Li J., Lin S., Yan H., He D. Detection and genetic characterization of Atypical Porcine Pestivirus in piglets with congenital tremors in Southern China. Front. Microbiol., 2019, 10: 1406 CrossRef
  39. Zhang K., Wu K., Liu J., Ge S., Xiao Y., Shang Y., Ning Z. Identification of atypical porcine pestivirus infection in swine herds in China. Transboundary and Emerging Diseases, 2017, 64(4): 1020-1023 CrossRef
  40. Zhou K., Yue H., Tang C., Ruan W., Zhou Q., Zhang B. Prevalence and genome characteristics of atypical porcine pestivirus in southwest China. Journal of General Virology,19, 100(1): 84-88 CrossRef
  41. Muñoz-González S., Canturri A., Pérez-Simó M., Bohórquez J.A., Rosell R., Cabezón O., Segalés J., Domingo M., Ganges L. First report of the novel atypical porcine pestivirus in Spain and a retrospective study. Transboundary and Emerging Diseases, 2017, 64(6): 1645-1649 CrossRef
  42. Kim S., Jeong C., Yoon S. Lee K., Yang M., Kim B., Lee S., Kang S., Kim W. Detection of atypical porcine pestivirus (APPV) from a case of congenital tremor in Korea. Korean J. Vet.Sci., 2017, 40: 209-213 CrossRef
  43. Mósena A.C.S., Weber M.N., da Cruz R.A.S., Cibulski S.P., da Silva M.S., Puhl D.E., Hammerschmitt M.E., Takeuti K.L., Driemeier D, de Barcellos D.E.S.N., Canal C.W. Presence of atypical porcine pestivirus (APPV) in Brazilian pigs. Transboundary and Emerging Diseases, 2018, 65(1): 22-26 CrossRef
  44. Mósena A.C.S., Weber M.N., Cibulski S.P., Silva M.S., Paim W.P., Silva G.S., Medeiros A.A., Viana N.A., Baumbach L.F., Puhl D.E., Silveira S., Corbellini L.G., Canal C.W. Survey for pestiviruses in backyard pigs in southern Brazil. Journal of Veterinary Diagnostic Investigation, 2020, 32(1): 136-141 CrossRef
  45. Possatti F., Headley S.A., Leme R.A., Dall Agnol A.M., Zotti E., de Oliveira T.E.S., Alfieri A.F., Alfieri A.A. Viruses associated with congenital tremor and high lethality in piglets. Transboundary Emerging Diseases, 2018, 65(2): 331-337 CrossRef
  46. Williamson S. Congenital tremor associated with atypical porcine pestivirus. Veterinary Record, 2017, 180(2): 42-43 CrossRef
  47. Postel A., Meyer D., Cagatay G.N., Feliziani F., De Mia G.M., Fischer N., Grundhoff A., Milićević V., Deng M.C., Chang C.Y., Qiu H.J., Sun Y., Wendt M., Becher P. High abundance and genetic variability of atypical porcine pestivirus in pigs from Europe and Asia. Emerging Infectious Diseases, 2017, 23(12): 2104-2107 CrossRef
  48. Dessureault F.G., Choinière M., Provost C., Gagnon C.A. First report of atypical porcine pestivirus in piglets with congenital tremor in Canada. Can. Vet. J., 2018, 59(4): 429-432.
  49. Yuan F., Feng Y., Bai J., Liu X., Arruda B., Anbalagan S., Peddireddi L. Genetic diversity and prevalence of Atypical Porcine Pestivirus in the Midwest of US swine herds during 2016-2018. Transboundary and Emerging Diseases, 2022, 69(2): 753-763 CrossRef
  50. Dénes L., Biksi I., Albert M., Szeredi L., Knapp D.G., Szilasi A., Bálint Á., Balka G. Detection and phylogenetic characterization of atypical porcine pestivirus strains in Hungary. Transboundary and Emerging Diseases, 2018, 65(6): 2039-2042 CrossRef
  51. Kasahara-Kamiie M., Kagawa M., Shiokawa M., Sunaga F., Fukase Y., Aihara N., Shiga T., Kamiie J., Aoki H., Nagai M. Detection and genetic analysis of a novel atypical porcine pestivirus from piglets with congenital tremor in Japan. Transboundary and Emerging Diseases, 2021, 69(4): 1761-1769 CrossRef
  52. Sozzi E., Salogni C., Lelli D., Barbieri I., Moreno A., Alborali G.L., Lavazza A. Molecular survey and phylogenetic analysis of atypical porcine pestivirus (APPV) identified in swine and wild boar from Northern Italy. Viruses, 2019, 11(12): 1142 CrossRef
  53. Stenberg H., Leveringhaus E., Malmsten A., Dalin A.M., Postel A., Malmberg M. Atypical porcine pestivirus — a widespread virus in the Swedish wild boar population. Transboundary and Emerging Diseases, 2021, 69(4): 2349-2360 CrossRef
  54. Kaufmann C., Stalder H., Sidler X., Renzullo S., Gurtner C., Grahofer A., Schweizer M. Long-term circulation of atypical porcine pestivirus (APPV) within Switzerland. Viruses, 2019, 11(7): 653 CrossRef
  55. Pedersen K., Kristensen C.S., Strandbygaard B., Botner A., Rasmussen T.B. Detection of atypical porcine pestivirus in piglets from Danish sow herds. Viruses, 2021, 13(5): 717 CrossRef
  56. Postel A., Hansmann F., Baechlein C., Fischer N., Alawi M., Grundhoff A., Derking S., Tenhündfeld J., Pfankuche V.M., Herder V., Baumgärtner W., Wendt M., Becher P. Presence of atypical porcine pestivirus (APPV) genomes in newborn piglets correlates with congenital tremor. Sci. Rep., 2016, 6: 27735 CrossRef
  57. Michelitsch A., Dalmann A., Wernike K., Reimann I., Beer M. Seroprevalences of newly discovered porcine pestiviruses in German pig farms. Vet. Sci., 2019, 6(4): 86 CrossRef
  58. Beer M., Wernike K., Dräger C., Höper D., Pohlmann A., Bergermann C., Schröder C., Klinkhammer S., Blome S., Hoffmann B. High prevalence of highly variable atypical porcine pestiviruses found in Germany. Transboundary and Emerging Diseases, 2017, 64(5): 22-26 CrossRef
  59. Stenberg H., Jacobson M., Malmberg M. Detection of atypical porcine pestivirus in Swedish piglets with congenital tremor type A-II. BMC Vet. Res., 2020, 16(1): 260 CrossRef
  60. Choe S., Park G.N., Cha R.M., Hyun B.H., Park B.K., An D.J. Prevalence and genetic diversity of atypical porcine pestivirus (APPV) detected in South Korean wild boars. Viruses, 2020, 12(6): 680 CrossRef
  61. Colom-Cadena A., Ganges L., Muñoz-González S., Castillo-Contreras R., Bohórquez J.A., Rosell R., Segalés J., Marco I., Cabezon O. Atypical porcine pestivirus in wild boar (Sus scrofa), Spain. Veterinary Record, 2018, 183(18): 569 CrossRef
  62. Cagatay G.N., Antos A., Meyer D., Maistrelli C., Keuling O., Becher P., Postel A. Frequent infection of wild boar with atypical porcine pestivirus (APPV). Transboundary and Emerging Diseases, 2018, 65(4): 1087-1093 CrossRef
  63. Pan S., Yan Y., Shi K., Wang M., Mou C., Chen Z. Molecular characterization of two novel atypical porcine pestivirus (APPV) strains from piglets with congenital tremor in China. Transboundary and Emerging Diseases, 2019, 66(1): 35-42 CrossRef
  64. Liu J., Li Z., Ren X., Li H., Lu R., Zhang Y., Ning Z. Viral load and histological distribution of atypical porcine pestivirus in different tissues of naturally infected piglets. Archives of Virology, 2019, 164(10): 2519-2523 CrossRef
  65. Shi K., Xie S., Sun W., Liu H., Zhao J., Yin Y., Si H., Qu S., Lu W. Evolution and genetic diversity of atypical porcine pestivirus (APPV) from piglets with congenital tremor in Guangxi Province, Southern China. Vet. Med. Sci., 2021, 7(3): 714-723 CrossRef
  66. Yin Y., Shi K., Sun W., Mo S. Complete genome sequence of an atypical porcine pestivirus strain, GX01-2018, from Guangxi Province, China. Microbiology Resource Announcements, 2019, 8(6): e01440-18 CrossRef
  67. Yuan F., Wang L. Genotyping atypical porcine pestivirus using NS5a. Infection, Genetics and Evolution, 2021, 92: 104866 CrossRef
  68. Jo W.K., van Elk C., van de Bildt M., van Run P., Petry M., Jesse S.T., Jung K., Ludlow M., Kuiken T., Osterhaus A. An evolutionary divergent pestivirus lacking the Npro gene systemically infects a whale species. Emerging Microbes and Infection, 2019, 8(1): 1383-1392 CrossRef
  69. Blome S., Beer M., Wernike K. New leaves in the growing tree of Pestiviruses. Advances in Virus Research, 2017, 99: 139-160 CrossRef
  70. Chen Z., Rijnbrand R., Jangra R.K., Devaraj S.G., Qu L., Ma Y., Lemon S.M., Li K. Ubiquitination and proteasomal degradation of interferon regulatory factor-3 induced by Npro from a cytopathic bovine viral diarrhea virus. Virology, 2007, 366: 277-292 CrossRef
  71. Riedel C., Aitkenhead H., El Omari K., Rümenapf T. Atypical porcine pestiviruses: relationships and conserved structural features. Viruses, 2021, 13(5): 760 CrossRef
  72. Bauhofer O., Summerfield A., Sakoda Y., Tratschin J.D., Hofmann M.A, Ruggli N. Classical swine fever virus Npro interacts with interferon regulatory factor 3 and induces its proteasomal degradation. Journal of Virology, 2007, 81(7): 3087-3096 CrossRef
  73. Mou C., Pan S., Wu H., Chen Z. Disruption of interferon-β production by the Npro of atypical porcine pestivirus. Virulence, 2021, 12(1): 654-665 CrossRef
  74. Liu J., Li Z., Ren X., Li H., Lu R., Zhang Y., Ning Z. Viral load and histological distribution of atypical porcine pestivirus in different tissues of naturally infected piglets. Archives of Virology, 2019, 164(10): 2519-2523 CrossRef
  75. Krey T., Bontems F., Vonrhein C., Vaney M.C., Bricogne G., Rümenapf T., Rey F.A. Crystal structure of the pestivirus envelope glycoprotein E(rns) and mechanistic analysis of its ribonuclease activity. Structure, 2012, 20(5): 862-873 CrossRef
  76. Cagatay G.N., Meyer D., Wendt M., Becher P., Postel A. Characterization of the humoral immune response induced after infection with atypical porcine pestivirus (APPV). Viruses, 2019, 11(10): 880 CrossRef
  77. Liu J., Zhang P., Chen Y., Zhong W., Li B., Pi M., Ning Z. Vaccination with virus-like particles of atypical porcine pestivirus inhibits virus replication in tissues of BALB/c mice. Archives of Virology, 2021, 6(10): 2733-2741 CrossRef
  78. Alekseev K.P., Raev S.A., Yuzhakov A.G., Shemel’kov E.V., Latyshev O.E., Eliseeva O.V., Kostina L.V., Tsibezov V.V., Stafford V.V., Kunakov K.Yu., Verkhovskiy O.A., Zaberezhnyy A.D., Aliper T.I. Experimental subunit vaccine against classical swine fever development and trial. Sel'skokhozyaistvennaya biologiya [Agricultural Biology], 2019, 54(6): 1236-1246 CrossRef
  79. Zhang H., Wen W., Hao G., Chen H., Qian P., Li X. A subunit vaccine based on E2 protein of atypical porcine pestivirus induces Th2-type immune response in mice. Viruses, 2018, 10(12): 673 CrossRef
  80. Li Y., Wang J., Kanai R., Modis Y. Crystal structure of glycoprotein E2 from bovine viral diarrhea virus. Proceeding of the National Academy of Sciences, 2013, 110(17): 6805-6810 CrossRef
  81. El Omari K., Iourin O., Harlos K., Grimes J.M., Stuart D.I. Structure of a pestivirus envelope glycoprotein E2 clarifies its role in cell entry. Cell Reports, 2013, 3(1): 30-35 CrossRef
  82. Krey T., Himmelreich A., Heimann M., Menge C., Thiel H.J., Maurer K., Rümenapf T. Function of bovine CD46 as a cellular receptor for bovine viral diarrhea virus is determined by complement control protein. Journal of Virology, 2006, 80(8): 3912-3922 CrossRef
  83. Drager C., Beer M., Blome S. Porcine complement regulatory protein CD46 and heparan sulfates are the major factors for classical swine fever virus attachment in vitro. Archives of Virology, 2015, 160(3): 739-746 CrossRef
  84. Cagatay G.N., Antos A., Suckstorff O., Isken O., Tautz N., Becher P., Postel A. Porcine complement regulatory protein CD46 is a major receptor for atypical porcine pestivirus but not for classical swine fever virus. Journal of Virology, 2021, 95: e02186-20 CrossRef
  85. Pan S., Mou C., Chen Z. An emerging novel virus: Atypical porcine pestivirus (APPV). Rev. Med. Virol., 2019, 29(1): e2018 CrossRef
  86. Pfankuche V., Hahn K., Bodewes R., Hansmann F., Habierski A., Haverkamp A.-K., Pfaender S., Walter S., Baechlein C., Postel A., Steinmann E., Becher P. Osterhaus A., Baumgärtner W., Puff C. Comparison of different in situ hybridization techniques for the detection of various RNA and DNA. Viruses, 2018, 10(7): 384 CrossRef
  87. Postel A., Meyer D., Petrov A., Becher P. Recent emergence of a novel porcine pestivirus: interference with classical swine fever diagnosis? Emerging Microbes and Infection, 2017, 6(4): e19 CrossRef

 

back

 


CONTENTS

 

 

Full article PDF (Rus)

Full article PDF (Eng)